Last synced on 14 November 2025 at 11:06 pm

ANGIOMED INTRODUCING SETS

Page Type
Cleared 510(K)
510(k) Number
K874771
510(k) Type
Traditional
Applicant
ANGIOMED U.S., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/12/1988
Days to Decision
54 days

ANGIOMED INTRODUCING SETS

Page Type
Cleared 510(K)
510(k) Number
K874771
510(k) Type
Traditional
Applicant
ANGIOMED U.S., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/12/1988
Days to Decision
54 days